intestinal edema Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Accumulation of cell free, noninflammatony fluid within the wall of the intestinal tract producing uniform thickening of the mucosal folds. (Human Phenotype Ontology, HP_0005225)
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2 genes associated with the intestinal edema phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
F12 coagulation factor XII (Hageman factor)
SERPING1 serpin peptidase inhibitor, clade G (C1 inhibitor), member 1